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Catalog Number:
03998
CAS Number:
34695-46-0
N-Boc-N-trifluoroacetyl-L-lysine N-hydroxysuccinimide ester
Purity:
≥ 98%
Synonym(s):
Boc-L-Lys(Tfa)-OSu
Documents
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Product Information

Na-Boc-Ne-trifluoroacetyl-L-lysine N-hydroxysuccinimide ester is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This compound features a unique trifluoroacetyl group, which enhances its reactivity and stability, making it an ideal choice for researchers looking to modify peptides or proteins with precision. Its N-hydroxysuccinimide ester functionality allows for efficient coupling reactions, facilitating the formation of stable amide bonds with various nucleophiles.

In the pharmaceutical and biotechnology industries, this compound is particularly valuable for developing targeted drug delivery systems and creating bioconjugates for diagnostic applications. Its ability to selectively modify amino acids in peptides opens up new avenues for the design of therapeutics with improved efficacy and reduced side effects. Researchers can leverage Na-Boc-Ne-trifluoroacetyl-L-lysine N-hydroxysuccinimide ester to streamline their synthesis processes and enhance the functionality of their biomolecules, making it a crucial tool in modern chemical biology.

Synonyms
Boc-L-Lys(Tfa)-OSu
CAS Number
34695-46-0
Purity
≥ 98%
Molecular Formula
C17H24F3N3O7
Molecular Weight
439.39
MDL Number
MFCD00038649
PubChem ID
294908
Melting Point
120-126 °C
Optical Rotation
[a]D25 = -24 ± 2º (C=1 in Acetone)
Conditions
Store at 0-8°C
General Information
Synonyms
Boc-L-Lys(Tfa)-OSu
CAS Number
34695-46-0
Purity
≥ 98%
Molecular Formula
C17H24F3N3O7
Molecular Weight
439.39
MDL Number
MFCD00038649
PubChem ID
294908
Melting Point
120-126 °C
Optical Rotation
[a]D25 = -24 ± 2º (C=1 in Acetone)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Boc-Ne-trifluoroacetyl-L-lysine N-hydroxysuccinimide ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures for therapeutic applications.
  • Drug Development: It is used in the development of novel drug candidates, particularly in the field of oncology, where targeted therapies are essential for effective treatment.
  • Bioconjugation: The compound facilitates bioconjugation processes, enabling the attachment of drugs to antibodies or other biomolecules, enhancing drug delivery and efficacy.
  • Protein Modification: It allows for specific modifications of proteins, which can be crucial for studying protein function and interactions in various biological systems.
  • Research in Immunology: This chemical plays a role in immunological studies, helping to create vaccines or immunotherapies by modifying antigens for better immune response.

Citations